Recruiting

Adenosine vs. Diltiazem

Sponsor:

University of Iowa

Code:

NCT07086560

Conditions

Supraventricular Tachycardia (SVT)

Eligibility Criteria

Sex: All

Age: 18 - 70+

Healthy Volunteers: Not accepted

Interventions

IV adenosine

IV diltiazem

Study Details

Brief summary:

Supraventricular tachycardia (SVT) is a dysrhythmia characterized rapid heart rate, typically with rapid onset. SVT accounts for over 50,000 emergency department visits per year. Of patients with regular, narrow-complex SVT, the mainstay of therapy includes adenosine and diltiazem. Adenosine is recommend by American and European guidelines as first-line therapy, however adenosine carries unique side effects that are potentially distressing to patients, including: "feeling of impending death or doom", flushing, anxiety, shortness of breath, and chest discomfort. Diltiazem does not carry this side effect profile, but has typically been reserved as second-line treatment due to side effects of low blood pressure associated with this class of medications. Diltiazem and adenosine have not been well studied head-to-head to compare safety and efficacy of their treatment for SVT. The purpose of this study is to evaluate safety and efficacy of adenosine and diltiazem for SVT in the ED (as completed through chart review of specific patient-level outcomes) and capture patient and clinician perspectives of medication satisfaction (through administration of questionnaires).

Conditions

Supraventricular Tachycardia (SVT)

Study ID

NCT07086560

Start date

Apr 4, 2025

Status verified date

Aug, 2026

Completion date

Dec, 2027

Anticipated

Primary completion date

Jun, 2027

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18 - 70+

Healthy Volunteers: Not accepted

Inclusion Criteria:

1. ED encounter for acute SVT
2. Age >/= 18 years
3. Receipt of IV adenosine and/or IV diltiazem for SVT in the ED or prehospital setting

Exclusion Criteria:

1. Neurologic status precluding survey participation due to medical instability
2. Pregnant
3. Incarcerated
4. Non-English speaking

Study Design

Enrollment

100 participants

Anticipated

Interventions and Outcome Measures

Arms

Adenosine

Diltiazem

Interventions

IV adenosine

Patients will not be randomized to intervention but will be categorized based on the exposure of IV adenosine for treatment of SVT received prior to study enrollment

IV diltiazem

Patients will not be randomized to intervention but will be categorized based on the exposure of IV diltiazem for treatment of SVT received prior to study enrollment

Primary outcome measure

  • Patient satisfaction with SVT treatment [ Time Frame: Primary outcome will be assessed during ED visit ]

Central Contacts and Locations

Central contacts

Locations

University of Iowa Health Care

Recruiting

Iowa City, Iowa, United States, 52242

Contacts

More Information

Sponsor

University of Iowa

Last update posted

Aug 21, 2026

Last verified

Aug, 2026

Keywords

  • diltiazem
  • adenosine
  • emergency medicine
  • supraventricular tachycardia

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-09. This information was provided to ClinicalTrials.gov by University of Iowa on 2026-08-21.